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GREEN Walk: A Nature-based Gait Training to Improve the Quality of Life Among Chronic Stroke Survivors

3 juni 2026 bijgewerkt door: Mary Audrey D. Viloria, Mariano Marcos State University

The purpose of the study is to find out if a nature-based gait training program titled GREEN Walk can help people with chronic stroke improve their physical, mental, and social health, as well as their overall quality of life. The participants in this study are people with chronic stroke who are able to take-part in walking rehabilitation. they will take part in a structured walking program designed to simulate real-life outdoor movement.

Participants will:

  1. Join GREEN Walk sessions that last about 60 minutes each.
  2. Walk through different natural-like environments with different terrains and simple obstacles.
  3. Perform guided walking tasks that challenge balance, strength, and coordination.
  4. Complete assessment tests before and after the program to measure changes in movement, mood, social participation, and overall health related quality of life.

The GREEN Walk program uses nature-based and varied walking activities to help participants practice real-world movement in a safe and structured way. Researchers will use the results of this study to understand whether this type of rehabilitation can support recovery and improve daily life after stroke.

Studie Overzicht

Toestand

Voltooid

Interventie / Behandeling

Gedetailleerde beschrijving

This study examined the effects of a structured, nature-based gait rehabilitation program titled GREEN Walk (Guided Recovery Engaging in Environment Walk) on physical, mental, social, and health-related quality of life outcomes among chronic stroke survivors. Chronic stroke is often associated with long-term impairments in mobility, emotional health, social participation, and overall functioning. Although conventional rehabilitation improves recovery in the early stages, many individuals reach a plateau in the chronic phase, where gains become limited despite ongoing deficits. This study explored whether integrating gait training with natural and functionally meaningful environments could provide additional benefits beyond traditional clinic-based approaches.

GREEN Walk was designed based on the understanding that walking is a complex activity requiring not only muscle strength and balance, but also attention, environmental awareness, emotional engagement, and adaptive motor control. Unlike conventional treadmill or indoor gait training, this program exposed participants to varied walking environments that simulate real-world conditions. These included level and uneven surfaces, ramps, curbs, stairs, and obstacle-based pathways that required continuous adjustment of posture, step strategy, and balance control. The progressive structure of the program aimed to challenge participants safely while promoting functional movement relevant to daily community ambulation.

The primary objective of the study was to determine the effects of GREEN Walk on four key domains of recovery: physical function, mental well-being, social participation, and overall health-related quality of life (HRQoL) in individuals with chronic stroke.

For physical outcomes, the intervention focused on improving gait performance, balance, lower extremity strength, coordination, and endurance. Chronic stroke survivors often experience reduced confidence in walking due to instability and fear of falling, leading to compensatory movement patterns and limited community mobility. Through repeated exposure to progressively challenging walking tasks, GREEN Walk promoted neuromuscular adaptation, improved postural control, and enhanced functional mobility. These improvements are essential for independence in daily activities such as walking outdoors, navigating uneven terrain, and performing community-based tasks.

In terms of mental health outcomes, the study assessed changes in emotional well-being, including stress, anxiety, mood, and motivation. Stroke survivors commonly experience psychological challenges such as reduced confidence, emotional distress, and frustration related to long-term disability. The integration of natural or nature-like environments was intended to reduce psychological stress and enhance emotional engagement during rehabilitation. Although some participants initially experienced increased emotional awareness during early sessions, likely reflected in short-term changes in DASS scores, continued participation led to improved psychological adaptation, reduced distress, and enhanced motivation by the end of the intervention period.

Regarding social participation, the study evaluated changes in the ability and willingness of participants to engage in social and community activities. Stroke-related mobility limitations often lead to social withdrawal and reduced interaction with others. While GREEN Walk showed a positive trend toward improved social participation, changes were not statistically significant within the six-week period. This suggests that while physical gains and increased confidence may begin to support social reintegration, longer intervention durations may be required to produce measurable improvements in this domain.

The study also assessed health-related quality of life (HRQoL) as a composite outcome reflecting physical, mental, and social well-being. Improvements were observed across multiple SF-36 domains, particularly after six weeks of intervention. Early gains were seen in physical role functioning, while more comprehensive improvements emerged later in areas such as physical functioning, energy and fatigue, emotional well-being, social functioning, general health, and perceived health change. These findings suggest that sustained exposure to nature-based gait training can produce cumulative benefits that extend beyond physical recovery to influence overall life satisfaction and daily functioning.

The intervention was implemented over a six-week period, with participants attending structured sessions three times per week. Each session lasted approximately 60 minutes and included warm-up exercises, a progressive walking program, and a cool-down phase. The walking activities were systematically advanced across weeks, starting from level surface walking and progressing toward more complex tasks such as obstacle negotiation, curb walking, ramp navigation, zigzag pathways, and stair climbing. This progression allowed participants to gradually adapt to increasing physical and environmental demands while maintaining safety under supervision. All sessions were conducted by licensed physical therapists who monitored performance, ensured safety, and adjusted activities according to participant capacity.

Outcome measures were assessed at multiple time points, including baseline and follow-up evaluations across the intervention period. Standardized tools were used to measure physical performance (Short Physical Performance Battery or SPPB), mental health status (Depression Anxiety Stress Scale or DASS-21), social skills and participation (Social Skills Inventory Scale or SSIS), and health-related quality of life (SF-36). Data analysis showed significant improvements in physical function at all time points, with the greatest gains observed at six weeks. Mental health outcomes showed an initial increase in distress followed by significant improvement by the end of the intervention. Social outcomes demonstrated positive but non-significant changes. HRQoL showed significant and multidimensional improvements at six weeks, indicating a cumulative effect of the intervention.

Overall, the findings suggest that GREEN Walk is an effective nature-based rehabilitation approach that significantly improves physical function and health-related quality of life in chronic stroke survivors, while also contributing to gradual improvements in mental well-being. Social participation, although positively influenced, may require longer intervention duration to achieve statistically significant changes. The study supports the idea that rehabilitation should extend beyond clinic-based settings and incorporate real-world, environment-driven movement experiences that address both physical and psychosocial aspects of recovery.

In conclusion, GREEN Walk demonstrates that structured gait training within natural and varied environments can provide a holistic rehabilitation approach for chronic stroke survivors. The integration of physical challenges with environmental stimulation supports not only mobility recovery but also emotional resilience and improved quality of life. Future studies with larger sample sizes, control groups, and longer follow-up periods are recommended to further validate these findings and explore long-term outcomes, including community participation, adherence, and sustainability of improvements.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

11

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Ilocos Norte
      • Batac City, Ilocos Norte, Filippijnen, 2906
        • Mariano Marcos State University

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  • have provided informed consent

Exclusion Criteria:

  • with other comorbidities

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Experimental Group

The study was a quasi-experimental study with only one group. All participants in the group received a 1 hr./day x 3 days/week x 6 weeks of progressing Guided Recovery Engaging in ENvironment Walk training (GREEN Walk) in the green spaces. The gait training includes the following:

  1. walking in even surfaces
  2. walking in uneven surfaces
  3. walking on curbs
  4. walking on ramps
  5. stair climbing
The GREEN Walk training program emphasizes a nature-based gait training and environmental adaptability. The participants were exposed to grassy pathways, inclined surfaces, uneven grounds, natural slopes, and obstacle enriched environments that simulated real life community ambulation as the intervention primarily utilized naturally available environments and simple obstacles, making it practical for long term implementation beyond clinic-based care. This form of training more closely resembled daily mobility situations encountered outside the rehabilitation setting, making the intervention more task specific and functionally relevant. Specifically, all participants attended a 1 hr./day x 3 days/week x 6 weeks of progressing Guided Recovery Engaging in ENvironment Walk training (please see attached Study Protocol Appendix for the exercise protocol). No other interventions provided to the participants.
Andere namen:
  • GREEN Walk Exercise

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Changes From and Significant Difference in Participants' Health-Related Quality of Life (HRQoL) between Baseline and one-week and six weeks post-intervention.
Tijdsspanne: From enrollment to first and six weeks post-intervention.

Using the Short Form Health Survey (SF-36) with subscales on the following:

  1. general health
  2. physical
  3. mental
  4. social
  5. emotional

Participants achieved a response if they scored a total health score ranging from 0 (worst health) to 100 (best health).

From enrollment to first and six weeks post-intervention.

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Changes From and Significant Difference in Participants' Physical Ability between Baseline and one-week and six weeks post-intervention.
Tijdsspanne: From enrollment to first and six weeks post-intervention.

Participants' physical ability was assessed using the Short Physical Performance Battery (SPPB), which included the following test areas:

  1. balance,
  2. gait speed, and
  3. lower extremity strength

Each test is scored 0-4, with a total score ranging from 0 (greater functional limitation) to 12 (better mobility).

Note: Please see study protocol where the SPPB form was included for reference.

From enrollment to first and six weeks post-intervention.
Changes From and Significant Difference in Participants' Mental Capacity between Baseline and one-week and six weeks post-intervention.
Tijdsspanne: From enrollment to first and six weeks post-intervention.

Participants' mental capacity was measured using the DASS-21 form, which included the following scales:

  1. Depression
  2. Anxiety
  3. Stress

The form utilized a 4-point likert scale in assessing depression, anxiety and stress and is classified into normal, mild, moderate, severe, and extremely severe. This study utilized the DASS-21. Higher total score indicates greater severity of depression, anxiety, and stress.

From enrollment to first and six weeks post-intervention.
Changes From and Significant Difference in Participants' Social status between Baseline and one-week and six weeks post-intervention.
Tijdsspanne: From enrollment to first and six weeks post-intervention.

This study utilized the Social Skills Inventory Scale (SSIS) to measure participants' social status, which includes the following sections of the form:

  1. Verbal and non-verbal communication
  2. self-care,
  3. self-control, and
  4. relationship skills

The outcome measurement used key scoring from 0-2. total accumulated score of on the identified sections, which was a total of 52 items. For the total score, lower score indicates strong social skills while higher scores suggest of needing improvement in social skills.

From enrollment to first and six weeks post-intervention.

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Mary Audrey D Viloria, MS in Rehabilitation Science, Mariano Marcos State University

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

28 maart 2025

Primaire voltooiing (Werkelijk)

10 mei 2025

Studie voltooiing (Werkelijk)

15 mei 2025

Studieregistratiedata

Eerst ingediend

28 mei 2026

Eerst ingediend dat voldeed aan de QC-criteria

3 juni 2026

Eerst geplaatst (Werkelijk)

8 juni 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

8 juni 2026

Laatste update ingediend die voldeed aan QC-criteria

3 juni 2026

Laatst geverifieerd

1 juni 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • PT-002

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

The data that will be shared will be the group data based on the statistical analysis method that will be utilized in the study.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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